Use of Alkyl Carboxylic Acid Amides as Penetration Enhancers

ABSTRACT

Use of carboxamides of the formula (I) 
       R 1 —CO—NR 2 R 3   (I),
 
     in which
     R 1  represents C 3 -C 19 -alkyl,   R 2  represents C 1 -C 6 -alkyl and   R 3  represents H or C 1 -C 6 -alkyl
 
for promoting the penetration of agrochemical active substances into plants.

The invention relates to the use of N-monoalkyl- andN,N-dialkyl-alkylcarboxamides in plant protection compositions and plantprotection compositions comprising such compounds.

EP-A 0 453 899 discloses the use ofN,N-dimethyl-C₅-C₁₉-alkylcarboxamides as crystallization inhibitors forcertain azole fungicides, such as tebuconazole, which have a tendency tocrystallize.

Surprisingly, it has now been found that alkylcarboxamides are suitablefor increasing the penetration of agrochemical active substances acrossthe cuticle of the plant and therefore for increasing the biologicalactivity of plant protection compositions.

The present invention therefore relates to the use of carboxamides ofthe formula (I)

R¹—CO—NR²R³  (I)

in which

-   R¹ represents C₃-C₁₉-alkyl,-   R² represents C₁-C₆-alkyl and-   R³ represents H or C₁-C₆-alkyl

for promoting the penetration of agrochemical active substances intoplants.

-   R¹ is preferably an unbranched or branched, saturated or    unsaturated, especially preferably unbranched, saturated alkyl group    having 5 to 11 carbon atoms, very especially preferably n-heptyl or    n-nonyl.-   R² and R³ are preferably identical or different, especially    preferably identical, and an unbranched or branched, especially    preferably unbranched alkyl group having 1 to 4 carbon atoms, very    especially preferably methyl.

Especially preferred compounds of the formula (I) are therefore those ofthe formula (Ia)

R¹—CO—N(CH₃)₂  (Ia)

in which

-   R¹ has the abovementioned meanings.

The following are very especially preferred: N,N-dimethyl-n-hexanamide,N,N-dimethyl-n-octanamide, N,N-dimethyl-n-decanamide andN,N-dimethyl-n-dodecanamide, in particular N,N-dimethyl-n-octanamide andN,N-dimethyl-n-decanamide.

The compounds of the formula (I) are employed individually or in theform of mixtures. Preferred is not only the use of individual activesubstances but also the use of a mixture which is known under the tradenames Hallcomid, Genagen or Agnique and which consists on average of 5%(unless otherwise specified, all percentages are percent by weight)N,N-dimethyl-hexanamide, 50% N,N-dimethyl-octanamide, 40%N,N-dimethyl-decanamide and 5% N,N-dimethyl-dodecanamide.

The acid amides of the formula (I) are known and commercially available.

The amount of one or more compounds of the formula (I) for the useaccording to the invention in plant protection compositions can varywithin wide limits, depending on the active substance and theformulation type.

In a preferred embodiment, the acid amides of the formula (I) thusadditionally act as solvents, while in another, likewise preferredembodiment, they act as additives for improving the biological activity.A further possibility is also the use as a tank mix additive, i.e. theaddition to the spray mixture of the formulation and not as integralcomponent of the formulation, and the use of the formulation as mixingpartner for improving the biological activity of other agents as theresult of an enhanced penetration.

Plant protection compositions according to the invention, i.e. plantprotection compositions which, in accordance with the invention,comprise one or more acid amides (I) for increasing the penetration ofthe active substance into plants, preferably have the followingcomposition:

-   -   1 to 90%, especially preferably 5 to 50%, of one or more        agrochemical active substances,    -   1 to 90%, especially preferably 5 to 70%, of one or more acid        amides of the formula (I) and    -   0 to 98% of other additives.

If the acid amides of the formula (I) do not act as solvents, but aspure additives for promoting the penetration of active substances intoplants, they are preferably present in the plant protection compositionsaccording to the invention in an amount of from 1 to 30%, especiallypreferably from 5 to 20%, in particular from 5 to 10%.

Since the mechanism of action of the acid amides (I) as penetrants isintrinsically independent of the nature of the agrochemical activesubstance employed, it is possible to use all active substances whosebiological activity can be increased as the result of an enhancedpenetration into a crop plant or a harmful plant.

The following may be mentioned by preference: fungicides, bactericides,insecticides, acaricides, nematicides, herbicides, plant growthregulators, plant nutrients, repellents with systemic properties, andcontact-acting agents which are suitable as combination partners.

Furthermore preferred are systemic active substances, i.e. those whichare taken up by the plant via the leaves or the roots and which aretranslocated in the sap, the plant's transport system. Especiallypreferred active substances are those with a log P value of ≦4(determined as specified in EC Directive 79/831 Annex V. A8 by HPLC,gradient method, acetonitrile/0.1% aqueous phosphoric acid), inparticular those with a log P value of ≦4 and ≧0.1.

Examples of individual active substances are:

Fungicides:

2-phenylphenol; 8-hydroxyquinoline sulphate; acibenzolar-S-methyl;aldimorph; amidoflumet; ampropylfos; ampropylfos-potassium; andoprim;anilazine; azaconazole; azoxystrobin; benalaxyl; benalaxyl-M; benodanil;benomyl; benthiavalicarb-isopropyl; benzamacril; benzamacril-isobutyl;bilanafos; binapacryl; biphenyl; bitertanol; blasticidin-S; boscalid;bromuconazole; bupirimate; buthiobate; butylamine; calcium polysulphide;capsimycin; captafol; captan; carbendazim; carboxin; carpropamid;carvone; quinomethionate; chlobenthiazone; chlorfenazole; chloroneb;chlorothalonil; chlozolinate; clozylacon; cyazofamid; cyflufenamid;cymoxanil; cyproconazole; cyprodinil; cyprofuram; Dagger G; debacarb;dichlofluanid; dichlone; dichlorophen; diclocymet; diclomezine;dicloran; diethofencarb; difenoconazole; diflumctorim; dimethirimol;dimethomorph; dimoxystrobin; diniconazole; diniconazole-M; dinocap;diphenylamine; dipyrithione; ditalimfos; dithianon; dodine; drazoxolon;edifenphos; epoxiconazole; ethaboxam; ethirimol; etridiazole;famoxadone; fenamidone; fenapanil; fenarimol; fenbuconazole; fenfuram;fenhexamid; fenitropan; fenoxanil; fenpiclonil; fenpropidin;fenpropimorph; ferbam; fluazinam; flubenzimine; fludioxonil; flumetover;flumorph; fluoromide; fluoxastrobin; fluquinconazole; flurprimidol;flusilazole; flusulfamide; flutolanil; flutriafol; folpet; fosetyl-Al;fosetyl-sodium; fuberidazole; furalaxyl; furametpyr, furcarbanil;furmecyclox; guazatine; hexachlorobenzene; hexaconazole; hymexazol;imazalil; imibenconazole; iminoctadine triacetate; iminoctadinetris(albesilate); iodocarb; ipconazole; iprobenfos; iprodione;iprovalicarb; irumamycin; isoprothiolane; isovaledione; kasugamycin;kresoxim-methyl; mancozeb; maneb; meferimzone; mepanipyrim; mepronil;metalaxyl; metalaxyl-M; metconazole; methasulfocarb; methfuroxam;metiram; metominostrobin; metsulfovax; mildiomycin; myclobutanil;myclozolin; natamycin; nicobifen; nitrothal-isopropyl; noviflumuron;nuarimol; ofurace; orysastrobin; oxadixyl; oxolinic acid; oxpoconazole;oxycarboxin; oxyfenthiin; paclobutrazol; pefurazoate; penconazole;pencycuron; phosdiphen; phthalide; picoxystrobin; piperalin; polyoxins;polyoxorim; probenazole; prochloraz; procymidone; propamocarb;propanosine-sodium; propiconazole; propineb; proquinazid;prothioconazole; pyraclostrobin; pyrazophos; pyrifenox; pyrimethanil;pyroquilon; pyroxyfur; pyrrolnitrine; quinconazole; quinoxyfen;quintozene; silthiofam; simeconazole; spiroxamine; sulfur; tebuconazole;tecloftalam; tecnazene; tetcyclacis; tetraconazole; thiabendazole;thicyofen; thifluzamide; thiophanate-methyl; thiram; tioxymid;tolclofos-methyl; tolylfluanid; triadimefon; triadimenol; triazbutil;triazoxide; tricyclamide; tricyclazole; tridemorph; trifloxystrobin;triflumizole; triforine; triticonazole; uniconazole; validamycin A;vinclozolin; zineb; ziram; zoxamide;(2S)—N-[2-[4-[[3-(4-chlorophenyl)-2-propynyl]oxy]-3-methoxy-phenyl]ethyl]-3-methyl-2-[(methylsulfonyl)amino]butanamide;1-(1-naphthalenyl)-1H-pyrrole-2,5-dione;2,3,5,6-tetrachloro-4-(methylsulfonyl)pyridine;2-amino-4-methyl-N-phenyl-5-thiazolecarboxamide;2-chloro-N-(2,3-dihydro-1,1,3-trimethyl-1H-inden-4-yl)-3-pyridinecarboxamide;3,4,5-trichloro-2,6-pyridinedicarbonitrile; actinovate;cis-1-(4-chlorophenyl)-2-(1H-1,2,4-triazol-1-yl)-cycloheptanol; methyl1-(2,3-dihydro-2,2-dimethyl-1H-inden-1-yl)-1H-imidazole-5-carboxylate;monopotassium carbonate;N-(6-methoxy-3-pyridinyl)cyclopropanecarboxamide;N-butyl-8-(1,1-dimethylethyl)-1-oxa-spiro[4.5]decan-3-amine; sodiumtetracarbonate;N-(3′4′-dichloro-5-fluorobiphenyl-2-yl)-3-(difluoromethyl)-methyl-1H-pyrazole-4-carboxamide;and copper salts and preparations, such as Bordeaux mixture; copperhydroxide, copper naphthenate; copper oxychloride; copper sulphate;cufraneb; cuprous oxide; mancopper; oxine copper.

Bactericides:

bronopol, dichlorophen, nitrapyrin, nickel-dimethyldithiocarbamate,kasugamycin, octhilinone, furancarboxylic acid, oxytetracyclin,probenazole, streptomycin, tecloftalam, copper sulphate and other copperpreparations.

Insecticides/Acaridices/Nematicides:

1. Acetylcholinesterase (AChE) Inhibitors

1.1 carbamates (for example alanycarb, aldicarb, aldoxycarb, allyxycarb,aminocarb, azamethiphos, bendiocarb, benfuracarb, bufencarb, butacarb,butocarboxim, butoxycarboxim, carbaryl, carbofuran, carbosulfan,chloethocarb, coumaphos, cyanofenphos, cyanophos, dimetilan,ethiofencarb, fenobucarb, fenothiocarb, formetanate, furathiocarb,isoprocarb, metam-sodium, methiocarb, methomyl, metolcarb, oxamyl,pirimicarb, promecarb, propoxur, thiodicarb, thiofanox, triazamate,trimethacarb, XMC, xylylcarb)

1.2 organophosphates (for example acephate, azamethiphos, azinphos(-methyl, -ethyl), bromophos-ethyl, bromfenvinfos (-methyl),butathiofos, cadusafos, carbophenothion, chlorethoxyfos,chlorfenvinphos, chlormephos, chlorpyrifos (-methyl/-ethyl), coumaphos,cyanofenphos, cyanophos, chlorfenvinphos, demeton-S-methyl,demeton-S-methyl sulphone, dialifos, diazinon, dichlofenthion,dichlorvos/DDVP, dicrotophos, dimethoate, dimethylvinphos,dioxabenzofos, disulfoton, EPN, ethion, ethoprophos, etrimfos, famphur,fenamiphos, fenitrothion, fensulfothion, fenthion, flupyrazofos,fonofos, formothion, fosmethilan, fosthiazate, heptenophos, iodofenphos,iprobenfos, isazofos, isofenphos, isopropyl O-salicylate, isoxathion,malathion, mecarbam, methacrifos, methamidophos, methidathion,mevinphos, monocrotophos, naled, omethoate, oxydemeton-methyl, parathion(-methyl/-ethyl), phenthoate, phorate, phosalone, phosmet, phosphamidon,phosphocarb, phoxim, pirimiphos (-methyl/-ethyl), profenofos, propaphos,propetamphos, prothiofos, prothoate, pyraclofos, pyridaphenthion,pyridathion, quinalphos, sebufos, sulfotep, sulprofos, tebupirimfos,temephos, terbufos, tetrachlorvinphos, thiometon, triazophos,triclorfon, vamidothion)

2. Sodium Channel Modulators/Voltage-Dependent Sodium Channel Blockers

2.1 pyrethroids (for example acrinathrin, allethrin (d-cis-trans,d-trans), beta-cyfluthrin, bifenthrin, bioallethrin,bioallethrin-S-cyclopentyl-isomer, bioethanomethrin, biopermethrin,bioresmethrin, chlovaporthrin, cis-cypermethrin, cis-resmethrin,cis-permethrin, clocythrin, cycloprothrin, cyfluthrin, cyhalothrin,cypermethrin (alpha-, beta-, theta-, zeta-), cyphenothrin, DDT,deltamethrin, empenthrin (1R isomer), esfenvalerate, etofenprox,fenfluthrin, fenpropathrin, fenpyrithrin, fenvalerate, flubrocythrinate,flucythrinate, flufenprox, flumethrin, fluvalinate, fubfenprox,gamma-cyhalothrin, imiprothrin, kadethrin, lambda-cyhalothrin,metofluthrin, permethrin (cis-, trans-); phenothrin (1R-trans isomer),prallethrin, profluthrin, protrifenbute, pyresmethrin, resmethrin, RU15525, silafluofen, tau-fluvalinate, tefluthrin, terallethrin,tetramethrin (1R-isomer), tralomethrin, transfluthrin, ZXI 8901,pyrethrins (pyrethrum))

2.2 oxadiazines (for example indoxacarb)

3. Acetylcholine Receptor Agonists/Antagonists

3.1 Chloronicotinyls/neonicotinoids (for example acetamiprid,clothianidin, dinotefuran, imidacloprid, nitenpyram, nithiazine,thiacloprid, thiamethoxam)

3.2 nicotine, bensultap, cartap

4. Acetylcholine Receptor Modulators

4.1 spinosyns (for example spinosad)

5. GABA-Controlled Chloride Channel Antagonists

5.1 cyclodiene organochlorines (for example camphechlor, chlordane,endosulfan, gamma-HCH, HCH, heptachlor, lindane, methoxychlor)

5.2 fiprols (for example acetoprole, ethiprole, fipronil, vaniliprole)

6. Chloride Channel Activators

6.1 mectins (for example abamectin, avermectin, emamectin,emamectin-benzoate, ivermectin, milbemectin, milbemycin)

7. Juvenile Hormone Mimetics

(for example diofenolan, epofenonane, fenoxycarb, hydroprene, kinoprene,methoprene, pyriproxifen, triprene)

8. Ecdysone Agonists/Disruptors

8.1 diacylhydrazines (for example chromafenozide, halofenozide,methoxyfenozide, tebufenozide)

9. Chitin Biosynthesis Inhibitors

9.1 benzoylureas (for example bistrifluoron, chlofluazuron,diflubenzuron, fluazuron, flucycloxuron, flufenoxuron, hexaflumuron,lufenuron, novaluron, noviflumuron, penfluoron, teflubenzuron,triflumuron)

9.2 buprofezin

9.3 cyromazine

10. Inhibitors of Oxidative Phosphorylation, ATP Disruptors

10.1 diafenthiuron

10.2 organotin compounds (for example azocyclotin, cyhexatin,fenbutatin-oxide)

11. Uncoupler of Oxidative Phosphorylation by Interrupting the H ProtonGradient

11.1 pyrroles (for example chlorfenapyr)

11.2 dinitrophenols (for example binapacyrl, dinobuton, dinocap, DNOC)

12. Site-I Electron Transport Inhibitors

12.1 METIs (for example fenazaquin, fenpyroximate, pyrimidifcn,pyridaben, tebufenpyrad, tolfenpyrad)

12.2 hydramethylnon

12.3 dicofol

13. Site-II Electron Transport Inhibitors

13.1 rotenone

14. Site-III Electron Transport Inhibitors

14.1 acequinocyl, fluacrypyrim

15. Microbial Disruptors of the Insect Gut Membrane

Bacillus thuringiensis strains

16. Fat Synthesis Inhibitors

16.1 tetronic acids (for example spirodiclofen, spiromesifen)

16.2 tetramic acids [for example3-(2,5-dimethylphenyl)-8-methoxy-2-oxo-1-azaspiro[4.5]dec-3-en-4-ylethyl carbonate (also known as: carbonic acid,3-(2,5-dimethylphenyl)-8-methoxy-2-oxo-1-azaspiro[4.5]dec-3-en-4-ylethyl ester, CAS-Reg.-No.: 382608-10-8) and carbonic acid,cis-3-(2,5-dimethylphenyl)-8-methoxy-2-oxo-1-azaspiro[4.5]dec-3-en-4-ylethyl ester (CAS-Reg.-No.: 203313-25-1)]

17. Carboxamides

(for example flonicamid)

18. Octopaminergic Agonists

(for example amitraz)

19. Inhibitors of Magnesium-Stimulated ATPase

(for example propargite)

20. Phthalamides

(for exampleN²-[1,1-dimethyl-2-(methylsulphonyl)ethyl]-3-iodo-N¹-[2-methyl-4-[1,2,2,2-tetrafluoro-1-(trifluoromethyl)ethyl]phenyl]-1,2-benzenedicarboxamide(CAS-Reg.-No.: 272451-65-7), flubendiamide)

21. Nereistoxin Analogues

(for example thiocyclam hydrogen oxalate, thiosultap-sodium)

22. Biologicals, Hormones or Pheromones

(for example azadirachtin, Bacillus spec., Beauveria spec., codlemone,Metarrhizium spec., Paecilomyces spec., thuringiensin, Verticilliumspec.)

23. Active Compounds with Unknown or Unspecific Mechanisms of Action

23.1 fumigants (for example aluminium phosphide, methyl bromide,sulphuryl fluoride)

23.2 selective antifeedants (for example cryolite, flonicamid,pymetrozine)

23.3 mite growth inhibitors (for example clofentezine, etoxazole,hexythiazox)

23.4 amidoflumet, benclothiaz, benzoximate, bifenazate, bromopropylate,buprofezin, quinomethionate, chlordimeform, chlorobenzilate,chloropicrin, clothiazoben, cycloprene, cyflumetofen, dicyclanil,fenoxacrim, fentrifanil, flubenzimine, flufenerim, flutenzin,gossyplure, hydramethylnone, japonilure, metoxadiazone, petroleum,piperonyl butoxide, potassium oleate, pyrafluprole, pyridalyl,pyriprole, sulfluramid, tetradifon, tetrasul, triarathene, verbutin,

furthermore the compound 3-methylphenyl propylcarbamate (tsumacide Z),the compound3-(5-chloro-3-pyridinyl)-8-(2,2,2-trifluoroethyl)-8-azabicyclo[3.2.1]octane-3-carbonitrile(CAS-Reg.-No. 185982-80-3) and the corresponding 3-endo isomer(CAS-Reg.-No. 185984-60-5) (cf. WO 96/37494, WO 98/25923), andpreparations which contain insecticidally active plant extracts,nematodes, fungi or viruses.

Herbicides:

Anilides such as, for example, diflufenican and propanil; arylcarboxylicacids such as, for example, dichloropicolinic acid, dicamba andpicloram; aryloxyalkanoic acids such as, for example, 2,4-D, 2,4-DB,2,4-DP, fluoroxypyr, MCPA, MCPP and triclopyr; aryloxyphenoxy-alkanoicesters, such as, for example, diclofop-methyl, fenoxaprop-ethyl,fluazifop-butyl, haloxyfop-methyl and quizalofop-ethyl; azinones, suchas, for example, chloridazon and norflurazon; carbamates such as, forexample, chlorpropham, desmedipham, phenmedipham and propham;chloroacetanilides such as, for example, alachlor, acetochlor,butachlor, metazachlor, metolachlor, pretilachlor and propachlor;dinitroanilines such as, for example, oryzalin, pendimethalin andtrifluralin; diphenyl ethers such as, for example, acifluorfen, bifenox,fluoroglycofen, fomesafen, halosafen, lactofen and oxyfluorfen; ureassuch as, for example, chlortoluron, diuron, fluometuron, isoproturon,linuron and methabenzthiazuron; hydroxylamines such as, for example,alloxydim, clethodim, cycloxydim, sethoxydim and tralkoxydim;imidazolinones such as, for example, imazethapyr, imazamethabenz,imazapyr and imazaquin; nitriles such as, for example, bromoxynil,dichlobenil and ioxynil; oxyacetamides such as, for example, mefenacet;sulphonylureas such as, for example, amidosulfuron, bensulfuron-methyl,chlorimuron-ethyl, chlorsulfuron, cinosulfuron, metsulfuron-methyl,nicosulfuron, primisulfuron, pyrazosulfuron-ethyl,thifensulfuron-methyl, triasulfuron and tribenuron-methyl;thiocarbamates such as, for example, butylate, cycloate, di-allate,EPTC, esprocarb, molinate, prosulfocarb, thiobencarb and tri-allate;triazines such as, for example, atrazin, cyanazin, simazin, simetryne,terbutryne and terbutylazin; triazinones such as, for example,hexazinon, metamitron and metribuzin; others such as, for example,aminotriazole,4-amino-N-(1,1-dimethylethyl)-4,5-dihydro-3-(1-methylethyl)-5-oxo-1H-1,2,4-triazole-1-carboxamide,benfuresate, bentazone, cinmethylin, clomazone, clopyralid, difenzoquat,dithiopyr, ethofumesate, fluorochloridone, glufosinate, glyphosate,isoxaben, pyridate, quinchlorac, quinmerac, sulphosate and tridiphane.

Examples of plant growth regulators which may be mentioned arechlorcholin chloride, thidiazuron, cyclanilide, ethephon, benzyladenineand gibberellic acid, and examples of the safener groups which may bementioned are mefenpyr, isoxadifen and cloquintocct-mexyl.

Examples of plant nutrients which may be mentioned are conventionalinorganic or organic fertilizers for providing plants withmacronutrients and/or micronutrients.

Examples of repellents which may be mentioned are diethyltolylamide,ethylhexanediol and butopyronoxyl.

Preferred examples of fungicides are the strobilurin fungicides such as,for example,

And the azole fungicides such as

Preferred examples of fungicides which may be mentioned areprothioconazole, fluoxastrobin, trifloxystrobin, spiroxamine andtebuconazole.

Prothioconazole is especially preferred, if appropriate as a mixturewith one or more of the following active substances: spiroxamine,tebuconazole, fluoxastrobin, trifloxystrobin.

The formulation types which are suitable include all formulations whichare applied to plants or their propagation material. The methods usedfor preparing them are generally known to the skilled worker and forexample described in Winnacker-Küchler, “Chemische Technologie”[Chemical Technology], volume 7, C. Hanser Verlag Munich, 4th edition,1986; J. W. van Valkenburg, “Pesticide Formulations”, Marcel DekkerN.Y., 1973, K. Martens, “Spray Drying Handbook”, 3rd Ed. 1979, G.Goodwin Ltd.; London, or Mollet, Grubenmann, “Formulierungstechnik”[Formulation Technology], Wiley-VCH-Verlag, Weinheim, 2000.

Examples of formulation types are all those mentioned in the “Manual ondevelopment and use of FAO and WHO specifications for pesticides” (FAOand WHO, 2002, appendix E) (in each case using the GCPF formulationcodes with English abbreviation and name): AB Grain bait; AE Aerosoldispenser; AL Any other liquid; AP Any other powder; CF CapsuleSuspension for Seed Treatment; CG Encapsulated granule; CL Contactliquid or gel; CP Contact powder; CS Capsule suspension; DC Dispersibleconcentrate; DP Dustable powder; DS Powder for dry seed treatment; DTTablet for direct application; EC Emulsifiable concentrate; EDElectrochargeable liquid; EG Emulsifiable Granule; EO Emulsion, water inoil; EP emulsifiable powder, ES Emulsion for seed treatment; EWEmulsion, oil in water; FG Fine granule; FS Flowable concentrate forseed treatment; GF Gel for Seed Treatment; GG Macrogranule; GLEmulsifiable gel; GP Flo-dust; GR Granule; GS Grease; GW Water solublegel; HN Hot fogging concentrate; KK Combi-pack solid/liquid; KLCombi-pack liquid/liquid; KN Cold fogging concentrate; KP Combi-packsolid/solid; LA Lacquer; LS Solution for seed treatment; MEMicroemulsion; MG Microgranule; OD oil dispersion, OF Oil miscibleflowable concentrate/oil miscible suspension; OL Oil miscible liquid; OPOil dispersible powder, PA Paste; PC Gel or paste concentrate; POPour-on; PR Plant rodlet; PS Seed coated with a pesticide; PT Pellet; RBBait (ready for use); SA Spot-on; SC suspension concentrate, SDsuspension concentrate for direct application, SE Suspo-emulsion; SGWater soluble granule; SL Soluble concentrate; SO Spreading oil; SPWater soluble powder; SS Water soluble powder for seed treatment; STWater soluble tablet; SU Ultra-low volume (ULV) suspension; TB Tablet;TC Technical material; TK Technical concentrate; UL Ultra-low volume(ULV) liquid; VP Vapour releasing product; WG Water dispersiblegranules; WP Wettable powder; WS Water dispersible powder for slurryseed treatment; WT Water dispersible tablet; XX Others.

Liquid formulation types are preferred. These include the formulationtypes DC (GCPF formulation code for dispersible concentrate); EC (GCPFformulation code for emulsion concentrate); EW (GCPF formulation codefor oil-in-water emulsion); ES (GCPF formulation code for emulsion forseed treatment), FS (GCPF formulation code for multiphase concentratefor seed treatment), EO (GCPF formulation code for water-in-oilemulsion; ME (GCPF formulation code for microemulsion; SE (GCPFformulation code for suspo-emulsion); SL (GCPF formulation code forsoluble concentrate); CS (GCPF formulation code for capsule suspension)and AL (GCPF formulation code for ready-to-use liquid formulation, anyother liquids for undiluted use).

Emulsion concentrates (formulation type EC) are especially preferred.

Suitable additives which may be present in the formulations according tothe invention, preferably the liquid formulations according to theinvention, are all customary formulation adjuvants such as organicsolvents, antifoams, emulsifiers, dispersants, preservatives, acids andbases, colorants, fillers and also water.

Antifoams which are suitable are conventional antifoams which arepresent in formulations of agrochemical active substances. Exampleswhich may be mentioned are silicone oils, silicone oil dispersions,magnesium stearate, phosphinic and phosphonic acids, in particularFluowet PL 80®.

Suitable organic solvents are not only alkanecarboxamides, such as thoseof the formula (I), but also all customary organic solvents whichthoroughly dissolve the agrochemically active substances employed. Thefollowing may be mentioned as being preferred: aliphatic and aromatic,optionally halogenated hydrocarbons such as toluene, xylene, Solvesso®,mineral oils such as white spirit, petroleum, alkylbenzenes and spindleoil, furthermore tetrachloromethane, chloroform, methylene chloride anddichloromethane, and furthermore esters such as ethyl acetate, lactates,furthermore lactones such as butyrolactone, moreover lactams such asN-methylpyrrolidone, N-octylpyrrolidone, N-dodecylpyrrolidone,N-octylcaprolactam and N-methylcaprolactam, γ-butyrolactone,dimethylformamide and tributyl phosphate.

Preference is given to carboxamides of the formula (I). Especiallypreferred are N,N-dimethyl-n-octanamide and N,N-dimethyl-n-decanamideand their mixtures.

Suitable emulsifiers are conventionally used surface-active substanceswhich are present in formulations of agrochemically active substances.Examples which may be mentioned are ethoxylated nonylphenols,polyethylene glycol ethers of linear alcohols, end-capped andnon-end-capped alkoxylated linear and branched, saturated andunsaturated alcohols, reaction products of alkylphenols with ethyleneoxide and/or propylene oxide, ethylene oxide/propylene oxide blockcopolymers, polyethylene glycols and polypropylene glycols, furthermorefatty acid esters, end-capped and non-end-capped alkoxylated linear andbranched, saturated and unsaturated fatty acids, fatty acid polyglycolether esters, alkylsulphonates, alkyl sulphates, aryl sulphates,ethoxylated arylalkylphenols such as, for example tristyryl phenolethoxylate with an average of 16 ethylene oxide units per molecule,furthermore ethoxylated and propoxylated arylalkylphenols and sulphatedor phosphated arylalkylphenol ethoxylates or -ethoxy- and -propoxylates.Especially preferred are tristyrylphenol alkoxylates and fatty acidpolyglycol ether esters. Very especially preferred are tristyrylphenolethoxylates, tristyrylphenol ethoxy-propoxylates and castor oilpolyglycol ether esters, in each case individually or in mixtures. Ifappropriate, additives such as surfactants or esters of fatty acidswhich contribute to improving the biological activity may also be used.

Dispersants which can be used are all substances which areconventionally employed in plant protection compositions for thispurpose. In addition to the examples which are mentioned hereinabove asemulsifiers, the following may be mentioned by preference: natural andsynthetic, water-soluble polymers such as gelatin, starch and cellulosederivatives, in particular cellulose esters and cellulose ethers,furthermore polyvinyl alcohol, polyvinylpyrrolidone, polyacrylic acid,polymethacrylic and copolymers of (meth)acrylic acid and (meth)acrylicesters, and furthermore alkali-metal-hydroxide-neutralized copolymers ofmethacrylic acid and methacrylic esters.

Preservatives which can be used are all substances which areconventionally present in plant treatment compositions for this purpose.Examples which may be mentioned are Preventol® and Proxel®.

Colorants which are suitable are all inorganic or organic colorantswhich are conventionally used for the preparation of plant protectioncompositions. Examples which may be mentioned are titanium dioxide,carbon black, zinc oxide and blue pigments.

Fillers which are suitable are all substances which are conventionallyemployed in plant protection compositions for this purpose. Thefollowing may be mentioned by preference: inorganic particles, such ascarbonates, silicates and oxides with a mean particle size of from 0.005to 5 μm, especially preferably from 0.02 to 2 μm. Examples which may bementioned are silicon dioxide, what are known as highly dispersedsilica, silica gels, and natural and synthetic silicates andalumosilicates.

Suitable compounds which act as emulsion stabilizers and/orcrystallization inhibitors are all substances which are conventionallyemployed in plant protection compositions for this purpose.

The content of the individual components in the formulations accordingto the invention can be varied within a substantial range.

The preparation of the formulations according to the invention isaccomplished for example in such a manner that the components are mixedwith one another in the described ratios. If the agrochemical activesubstance is a solid, the latter is generally employed in finely groundform or in the form of a solution or suspension in an organic solvent orwater. If the agrochemical active substance is liquid, the use of anorganic solvent can frequently be dispensed with. Moreover, a solidagrochemical substance may be employed in the form of a melt.

When carrying out the process, the temperatures can be varied within acertain range. In general, the process is carried out at temperatures ofbetween 0° C. and 80° C., preferably between 10° C. and 60° C.

When carrying out the process according to the invention, a procedure isgenerally followed in which the acid amides (I) are mixed with one ormore active substances and, if appropriate, with additives. Thecomponents can be mixed with one another in any order.

The equipment which is suitable for carrying out the process accordingto the invention is customary equipment which is employed for thepreparation of agrochemical formulations.

Suitable application forms are all those methods which are known to theskilled worker as being conventionally used; examples which may bementioned are: spraying, immersion, misting and a series of specificmethods for the direct below- or above-ground treatment of whole plantsor parts (seeds, root, stolons, stalks, stem, leaf), such as, forexample, in the case of trees the injection into the stem or in the caseof perennial plants stalk bands, and a series of specific indirectapplication methods.

The specific application rate of the plant protection compositions of awide range of formulation types for controlling the abovementionedharmful organisms, either based on area and/or the object to be treatedvaries greatly. In general, the application media which are known to theskilled worker as being conventionally used for the field of applicationin question, are employed in customary amounts, such as, for example,from several hundred litres of water per hectare in the case of standardspray methods to a few litres of oil per hectare in the case of ‘UltraLow Volume’ aerial application to a few millilitres of a physiologicalsolution in the case of injection methods. The concentrations of theplant protection compositions according to the invention in the relevantapplication media therefore vary within a wide range and depend on thespecific field of application. In general, concentrations are used whichare known to the skilled worker as being conventionally used for thespecific field of application. Preferred concentrations are from 0.01%by weight to 99% by weight, especially preferred concentrations from0.1% by weight to 90% by weight.

The agrochemical formulations according to the invention, for example inthe use forms which are conventional for liquid preparations, can beapplied either as such or after previously having been diluted withwater, that is to say for example as emulsions, suspensions orsolutions. The application here is accomplished by the customarymethods, that is to say, for example, by spraying, pouring or injecting.

The application rate of the agrochemical formulations according to theinvention can be varied within a substantial range. It depends on theagrochemical active substances in question and on their content in theformulations.

The invention furthermore relates to a method of promoting thepenetration of agrochemical active substances into plants, theagrochemical active substance being applied to the plants eithersimultaneously or sequentially with one or more acid amides of theformula (I).

Some of the plant protection compositions according to the invention areknown and some are new.

The invention also relates to a plant protection composition comprising

-   -   a) 1 to 80% of one or more acid amides of the formula (I) as        stated above,    -   b) 1 to 90% of one or more agrochemical active substances and    -   c) 0 to 98% of additives,

the following agrochemical substances being excluded:

A. an azole derivative of the formula (II)

-   -   in which    -   a) R¹ represents

-   -   -   R² represents tert-butyl and        -   R³ represents hydroxyl,

    -   or

    -   b) R¹ represents 4-fluorophenyl,        -   R² represents 2-fluorophenyl and        -   R³ represents hydroxyl,

    -   or

    -   c) represents 2,4-dichlorophenyl,        -   R² represents n-butyl and        -   R³ represents hydroxyl,

    -   or

    -   d) R¹ represents

-   -   -   R² represents phenyl and        -   R³ represents cyano,

    -   or

    -   e) R¹ represents 2-chlorobenzyl,        -   R² represents 1-chlorocycloprop-1-yl

    -   and        -   R³ represents hydroxyl,

    -   or

    -   f) R¹ represents 4-chlorophenyl        -   R² represents

-   -   and        -   R³ represents hydroxyl,    -   and/or    -   an azole derivative of the formula (III)

-   -   in which    -   a) Y represents —CH(OH) and        -   R⁴ represents chlorine or phenyl,    -   or    -   b) Y represents CO and        -   R⁴ represents chlorine,    -   and/or    -   an azole derivative of the formula (IV)

-   -   in which    -   R⁵ represents hydrogen or chlorine,    -   and/or    -   1-[bis(4-fluorophenyl)methylsilyl]-1H-(1,2,4-triazole) of the        formula (V),

B. a carbamate of the formula (VI)

-   -   where    -   Ar represents an aryl group or a heterocyclic group, each of        which is optionally substituted,

and

-   -   R, R′ represent H or methyl; and

C. thiadiazuron.

The invention also relates to a plant protection composition comprising

-   a) 1 to 30%, preferably 5 to 20%, especially preferably 5 to 10%, of    one or more acid amides of the formula (I) as stated above,-   b) 1 to 90% of one or more agrochemical active substances and-   c) 0 to 98% of additives,

excluding tebuconazole and triadimenol as agrochemical activesubstances.

Preferred plant protection compositions according to the invention arethose which comprise prothioconazole as agrochemical active substance,if appropriate in mixture with further agrochemical active substances.

As regards the use of herbicides, the plants treated in accordance withthe invention are all weed species. As regards the protection of cropplants by the application of, for example, fungicides and insecticides,the use in economically important, including, for example, transgenic,crops of useful plants and ornamentals, for example cereals such aswheat, barley, rye, oats, sorghum and millet, rice, cassava and maize,or else crops of peanut, sugar beet, cotton, soya, oilseed rape, potato,tomato, pea and vegetables is preferred.

The invention is illustrated in greater detail by the examples withoutbeing limited thereto.

EXAMPLES Penetration Test

In this test, the measured quantity was the penetration of activesubstances across enzymatically isolated cuticles of apple tree leaves.

The leaves used were leaves which had been excised in the fullydeveloped state from cv. Golden Delicious. The cuticles were isolated insuch a way that

-   -   first, using the vacuum infiltration method, leaf discs which        had been marked with dye and punched from the underside were        filled with a pectinase solution (0.2 to 2% strength) which had        been buffered to a pH of between 3 and 4,    -   then, sodium azide was added and    -   the leaf discs treated thus were left to stand until the        original leaf structure had disintegrated and the noncellular        cuticle had detached itself.

Thereafter, only the cuticles of the upper side of the leaf which werefree from stomata and hairs were used. They were washed repeatedly,alternating with water and a buffer solution of pH 7. The resultingclean cuticles were finally applied to Teflon discs and smoothed anddried using a weak stream of air.

In the next step, the cuticle membranes obtained were placed intostainless-steel diffusion cells (=transport chambers) in order to carryout membrane transport studies. To this end, tweezers were used to placethe cuticles centrally on the edges of the diffusion cells which hadbeen painted with silicone fat and sealed using a ring, which had alsobeen painted with fat. The arrangement had been chosen in such a waythat the morphological external side of the cuticles was directedoutwardly, that is to say facing the air, while the original internalside faced the inside of the diffusion cell. The diffusion cells werefilled with water or with a mixture of water and solvent.

To determine the penetration, in each case 9 μl of a spray mixture ofthe composition mentioned in the examples were applied to the externalside of a cuticle.

In the spray mixtures, CIPAC water was used in each case.

After the spray mixtures had been applied, the water was left toevaporate in each case, and the chambers were then inverted and placedinto temperature-controlled cans, the external side of the cuticle beingflushed with air at a defined temperature and humidity. The beginning ofthe penetration therefore took place at a relative atmospheric humidityof 60% and a set temperature of 25° C. The penetration of the activesubstance was measured using a radiolabelled active substance.

As can be seen with reference to the examples in the table, the presenceof acid amides (in the present case N,N-dimethyldecanamide by way ofexample) gives rise to a substantially increased uptake in comparisonwith the formulations which lack the acid amides. The employedalternatives to the acid amide are examples of commercially availablesolvents for formulations.

Table, Example 1

The active substance is dissolved in an acetone/water mixture at aconcentration of 0.5 g/l, and the penetration is measured after 3 and 48hours.

Table, Example 2

The water is mixed together with formulation adjuvants andN,N-dimethyldecanamide and this mixture is diluted with water so thatthe dilution again contains an active substance concentration of 0.5g/l. As in Ex. 1, the penetration was then measured after 3 and 48hours.

Table, Example 3

The active substance is mixed together with formulation adjuvants andN-methylpyrrolidone and this mixture is diluted with water so that thedilution contains an active substance concentration of 0.5 g/l. Thepenetration was measured after 3 and 48 hours.

Table, Example 4

The active substance is mixed together with formulation adjuvants andγ-butyrolactone and this mixture is diluted with water so that thedilution contains an active substance concentration of 0.5 g/l. Thepenetration was measured after 3 and 48 hours.

Table, Example 5

The active substance is mixed together with formulation adjuvants andN,N-dimethyldecanamide and this mixture is diluted with water so thatthe dilution contains an active substance concentration of 1.0 g/l. Asin Ex. 1, the penetration was then measured after 3 and 48 hours.

Table, Example 6

The active substance is mixed together with formulation adjuvants andN-methylpyrrolidone and this mixture is diluted with water so that thedilution contains an active substance concentration of 1.0 g/l. Thepenetration was measured after 3 and 48 hours.

Table, Example 7

The active substance is mixed together with formulation adjuvants andγ-butyrolactone and this mixture is diluted with water so that thedilution contains an active substance concentration of 1.0 g/l. Thepenetration was measured after 3 and 48 hours.

Table, Example 8

The active substances prothioconazole and tebuconazole are mixedtogether with formulation adjuvants and N,N-dimethyldecanamide and thismixture is diluted with water so that the dilution contains aprothioconazole concentration of 0.5 g/l. The penetration was thenmeasured after 3 and 48 hours.

Table, Example 9

The active substances prothioconazole and tebuconazole are mixedtogether with formulation adjuvants and N-methylpyrrolidone and thismixture is diluted with water so that the dilution contains aprothioconazole concentration of 0.5 g/l. The penetration was thenmeasured after 3 and 48 hours.

Table, Example 10

The active substances prothioconazole and tebuconazole are mixedtogether with formulation adjuvants and γ-butyrolactone and this mixtureis diluted with water so that the dilution contains a prothioconazoleconcentration of 0.5 g/l. The penetration was then measured after 3 and48 hours.

Table, Example 11

The active substances prothioconazole and spiroxamine are mixed togetherwith formulation adjuvants and N,N-dimethyldecanamide and this mixtureis diluted with water so that the dilution contains a prothioconazoleconcentration of 0.5 g/l. The penetration was measured after 3 and 48hours.

Table, Example 12

The active substances prothioconazole and spiroxamine are mixed togetherwith formulation adjuvants and N-methylpyrrolidone and this mixture isdiluted with water so that the dilution contains a prothioconazoleconcentration of 0.5 g/l. The penetration was measured after 3 and 48hours.

Table, Example 13

The active substances prothioconazole and spiroxamine are mixed togetherwith formulation adjuvants and a mixture of aromatics (boiling point220-290° C.) and this mixture is diluted with water so that the dilutioncontains a prothioconazole concentration of 0.5 g/l. The penetration wasmeasured after 3 and 48 hours.

Penetration test, table % penetration % penetration (+/− SE) (+/− SE)Prothioconazole prothioconazole prothioconazole Ex- concentration (g/l)in after 3 h after 48 h ample Solvent Active substances the aqueousdilution n = 5-7 n = 5-7 1 Acetone (without further formulationprothioconazole 0.5  0.23 (0.06)  0.72 (0.17) adjuvants) 2N,N-Dimethyldecanamide prothioconazole 0.5  1.73 (0.45)  6.99 (1.23) 3N-Methylpyrrolidone prothioconazole 0.5  0.16 (0.04)  2.23 (0.49) 4gamma-Butyrolactone prothioconazole 0.5  0.12 (0.04)  1.4 (0.37) 5N,N-Dimethyldecanamide prothioconazole 1.0  1.24 (0.34)  6.82 (1.63) 6N-Methylpyrrolidone prothioconazole 1.0  0.18 (0.03)  1.57 (0.45) 7gamma-Butyrolactone prothioconazole 1.0  0.09 (0.03)  2.38 (1.29) 8N,N-Dimethyldecanamide prothioconazole & tebuconazole 0.5 13.13 (1.96)38.17 (6.78) 9 N-Methylpyrrolidone prothioconazole & tebuconazole 0.5 0.74 (0.12) 13.42 (1.36) 10 gamma-Butyrolactone prothioconazole &tebuconazole 0.5  0.67 (0.19)  13.9 (2.48) 11 N,N-Dimethyldecanamideprothioconazole & spiroxamine  0.5  8.08 (1.01) 28.69 (3.51) 12N-Methylpyrrolidone prothioconazole & spiroxamine  0.5  1.62 (0.28)17.79 (3.7)  13 Mixture of aromatics (*1) prothioconazole & spiroxamine 0.5 0.84 (0.3) 10.15 (4.59) Thidiazuron % penetration % penetrationconcentration thidiazuron thidiazuron Ex- Active (g/l) in the dilutionafter 1-1.5 h after 22 h ample Test substance (g/l) substances(acetone/water, 20/80) n = 5-7 n = 5-7 14 Active substance (without testsubstance) thidiazuron 0.5 <1 <1 15 N,N-Dimethyloctanamide/ thidiazuron0.5 37.7 43.1 decanamide**(3 g/l) 16 Hasten*** (2 g/l) thidiazuron 0.58.0 27.0 17 Hasten (10 g/l) thidiazuron 0.5 12.6 39.2 18 Agridex**** (10g/l) thidiazuron 0.5 1.44 46.6 BYF587 % penetration % penetrationconcentration (g/l) BYF587 BYF587 Ex- Formulation/test substance in inthe aqueous after 7 h after 26 h ample the spray mixture (g/l) Activesubstances dilution n = 5-7 n = 5-7 19 SC100 N-(3'4'-dichloro-5- 0.250.8 1.6 fluorobiphenyl-2-yl)-3- (difluoromethyl)-1-methyl-1H-pyrazole-4-carboxamide 20 EC200 / N,N- N-(3'4'-dichloro-5- 0.25 25.740.7 Dimethyldecanamide**(0.5 g/l) fluorobiphenyl-2-yl)-3-(difluoromethyl)-1-methyl- 1H-pyrazole-4-carboxamide 21 EC200 / N,N-N-(3'4'-dichloro-5- 0.25 38.9 54.3 Dimethyldecanamide**(1.5 g/l)fluorobiphenyl-2-yl)-3- (difluoromethyl)-1-methyl-1H-pyrazole-4-carboxamide (*1) boiling point: 220-290° C. **HallcomidM8-10 ***commercial tank mix additive with ethyl/methyl oleate as mainconstituent ****commercial tank mix additive, mineral oil concentrate

1. A method for promoting the penetration of one or more agrochemicalactive substances into plants, wherein said agrochemical activesubstances are selected from the group consisting of prothioconazole,N-(3′,4′-dichloro-5-fluorobiphenyl-2-yl)-3-(difluoromethyl)-1-methyl-1H-pyrazole-4-carboxamideand mixtures of prothioconazole and one or more active substancesselected from the group consisting of spiroxamine, tebuconazole,fluxastrobin and trifloxystrobin, comprising, applying to said plantsone or more carboxamides of the formula (I)R¹—CO—NR²R³  (I) in which R¹ represents an unbranched, saturated alkylgroup having 5 to 11 carbon atoms, R² represents C₁-C₆-alkyl, and R³represents H or C₁-C₆-alkyl.
 2. A method according to claim 1, whereinR² and R³ are methyl.
 3. A method according to claim 1, wherein saidcarboxamide is N,N-dimethyl n-octanamide or N,N-dimethyl n-decanamide.4. A method according to claim 1, wherein said one or more carboxamidesis a mixture of 5% N,N-dimethyl hexanamide, 50% N,N-dimethyl octanamide,40% N,N-dimethyl decanamide and 5% N,N-dimethyl dodecanamide, whereinthe percentages are percent by weight.
 5. (canceled)
 6. A methodaccording to claim 1, wherein said one or more carboxamides is appliedas an aqueous spray mixture.
 7. A method according to claim 1, whereinsaid one or more agrochemical active substances comprises a systemicagrochemical substance.
 8. (canceled)
 9. A method according to claim 1,wherein said one or more agrochemical active substances is selected fromthe group consisting of prothioconazole andN-(3′4′-dichloro-5-fluorobiphenyl-2-yl)-3-(difluoromethyl)-1-methyl-1H-pyrazole-4-carboxamide.10. A method according to claim 9, wherein said agrochemical activesubstance is prothioconazole.
 11. A method of promoting the penetrationof one or more agrochemical active substances into plants according toclaim 1, wherein said one or more agrochemical active substances, whichare selected from the group consisting of prothioconazole.N-(3′,4′-dichloro-5-fluorobiphenyl-2-yl)-3-(difluoromethyl)-1-methyl-1H-pyrazole-4-carboxamideand mixtures of prothioconazole and one or more active substancesselected from the group consisting of spiroxamine, tebuconazole,fluoxastrobin and trifloxystrobin, is applied to the plantssimultaneously or sequentially with said one or more carboxamides of theformula (I),R¹—CO—NR²R³  (I) wherein R¹ represents an unbranched, saturated alkylgroup having 5 to 11 carbon atoms, R² represents C₁-C₆-alkyl, and R³represents H or C₁-C₆-alkyl.
 12. A plant protection compositioncomprising, a) 1 to 80% of one or more carboxamides of the formula (I),R¹—CO—NR²R³  (I) wherein R¹ represents an unbranched, saturated alkylgroup having 5 to 11 carbon atoms, R² represents C₁-C₆-alkyl, and R³represents H or C₁-C₆-alkyl, b) 1 to 90% of one or more agrochemicalactive substances, which are selected from the group consisting ofprothioconazole,N-(3′,4′-dichloro-5-fluorobiphenyl-2-yl)-3-(difluoromethyl)-1-methyl-1H-pyrazole-4-carboxamideand mixtures of prothioconazole and one or more active substancesselected from the group consisting of spiroxamine, tebuconazole,fluoxastrobin and trifloxystrobin, and c) 0 to 98% of additives whereinthe percentages are percent by weight.
 13. A plant protectioncomposition comprising a) 1 to 30% of one or more carboxamides of theformula (I),R¹—CO—NR²R³  (I) wherein R¹ represents an unbranched, saturated alkylgroup having 5 to 11 carbon atoms, R² represents C₁-C₆-alkyl, and R³represents H or C₁-C₆-alkyl, b) 1 to 90% of one or more agrochemicalactive substances, which are selected from the group consisting ofprothioconazole,N-(3′,4′-dichloro-5-fluorobiphenyl-2-yl)-3-(difluoromethyl)-1-methyl-1H-pyrazole-4-carboxamideand mixtures of prothioconazole and one or more active substancesselected from the group consisting of spiroxamine, tebuconazole,fluoxastrobin and trifloxystrobin, and c) 0 to 98% of additives andwherein the percentages are percent by weight.
 14. A plant protectioncomposition according to claim 12, comprising, as agrochemical activesubstance, prothioconazole orN-(3′,4′-dichloro-5-fluorobiphenyl-2-yl)-3-(difluoromethyl)-1-methyl-1H-pyrazole-4-carboxamide.15. A plant protection composition according to claim 13, comprising, asagrochemical active substance, prothioconazole orN-(3′,4′-dichloro-5-fluorobiphenyl-2-yl)-3-(difluoromethyl)-1-methyl-1H-pyrazole-4-carboxamide.16. A method according to claim 1, wherein said one or more carboxamidesof the formula (I) are formulated into a plant protection compositioncomprising, a) 1 to 90% of one or more agrochemical active substances,which are selected from the group consisting of prothioconazole,N-(3′,4′-dichloro-5-fluorobiphenyl-2-yl)-3-(difluoromethyl)-1-methyl-1H-pyrazole-4-carboxamideand mixtures of prothioconazole and one or more active substancesselected from the group consisting of spiroxamine, tebuconazole,fluoxastrobin and trifloxystrobin, b) 1 to 90% of one or morecarboxamides of the formula (I), and c) 0 to 98% of other additiveswherein the percentages are percent by weight.
 17. The method accordingto claim 1 wherein said one or more agrochemical active substances is amixture of prothioconazole and tebuconazole.
 18. The method according toclaim 17 wherein said one or more carboxamides of formula (I) isN,N-dimethyl n-octanamide or N,N-dimethyl n-decanamide.
 19. The methodaccording to claim 18 wherein said one or more carboxamides of formula(I) is N,N-dimethyl n-decanamide.
 20. The method according to claim 1wherein said one or more agrochemical active substances is a mixture ofprothioconazole and spiroxamine.
 21. The method according to claim 20wherein said one or more carboxamides of formula (I) is N,N-dimethyln-octanamide or N,N-dimethyl n-decanamide.
 22. The method according toclaim 21 wherein said one or more carboxamides of formula (I) isN,N-dimethyl n-decanamide.
 23. The plant protection compositionaccording to claim 12 wherein said one or more agrochemical activesubstances is a mixture of prothioconazole and tebuconazole.
 24. Theplant protection composition according to claim 23 wherein said one ormore carboxamides of the formula (I) is N,N-dimethyl n-octanamide orN,N-dimethyl n-decanamide.
 25. The plant protection compositionaccording to claim 24 wherein said one or more carboxamides of formula(I) is N,N-dimethyl n-decanamide.
 26. The plant protection compositionaccording to claim 12 wherein said one or more agrochemical activesubstances is a mixture of prothioconazole and spiroxamine.
 27. Theplant protection composition according to claim 26 wherein said one ormore carboxamides of the formula (I) is N,N-dimethyl n-octanamide orN,N-dimethyl n-decanamide.
 28. The plant protection compositionaccording to claim 27 wherein said one or more carboxamides of formula(I) is N,N-dimethyl n-decanamide.
 29. The method according to claim 16wherein said one or more agrochemical active substances comprises amixture of prothioconazole and tebuconazole.
 30. The method according toclaim 29 wherein said one or more carboxamides of formula (I) isN,N-dimethyl n-octanamide or N,N-dimethyl n-decanamide.
 31. The methodaccording to claim 30 wherein said one or more carboxamides of formula(I) is N,N-dimethyl n-decanamide.
 32. The method according to claim 16wherein said one or more agrochemical active substances comprises amixture of prothioconazole and spiroxamine.
 33. The method according toclaim 32 wherein said one or more carboxamides of formula (I) isN,N-dimethyl n-octanamide or N,N-dimethyl n-decanamide.
 34. The methodaccording to claim 33 wherein said one or more carboxamides of formula(I) is N,N-dimethyl n-decanamide.